电催化剂
过渡金属
氮气
固氮
氧化还原
电子转移
固氮酶
金属
化学
溶解
密度泛函理论
氨生产
无机化学
光化学
电化学
物理化学
计算化学
催化作用
电极
有机化学
生物化学
作者
Nan Zhang,Yaping Gao,Lixia Ma,Yuyang Wang,Luo Huang,Baoqiang Wei,Yanzhong Xue,Houyu Zhu,Ruibin Jiang
标识
DOI:10.1016/j.ijhydene.2022.09.074
摘要
Electrocatalytic nitrogen reduction reaction (NRR) provides a green and sustainable way to produce ammonia at ambient conditions. The key to realize highly efficient NRR is the catalysts. To design highly active electrocatalysts for NRR, the multistep mechanism involved in NRR must be clearly unraveled. Herein, single V atoms anchored on g-C3N4 is identified to be an efficient electrocatalyst for NRR by screening single 3d transition metal (TM = Sc to Zn) atoms anchored by g-C3N4 ([email protected]3N4) through density functional theory calculations. NRR takes place on [email protected]3N4 preferentially through distal path with a relatively low limiting potential of −0.55 V. The outstanding NRR performance of [email protected]3N4 is found from the peculiar electronic structure of V after anchored in the six-fold cavity of g-C3N4 and the good transmitter role of V for electron transfer between NxHy species and g-C3N4. Moreover, the formation energy and dissolution potential indicate that [email protected]3N4 is thermodynamically and electrochemically stable and the aggregation of V atoms is unfavorable thermodynamically, signifying that the synthesis of [email protected]3N4 is feasible in experiments. Our work screens out a superior noble metal-free NRR electrocatalyst and will be helpful for the development of ambient artificial nitrogen fixation.
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